JP2010519181A5 - - Google Patents
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- JP2010519181A5 JP2010519181A5 JP2009548468A JP2009548468A JP2010519181A5 JP 2010519181 A5 JP2010519181 A5 JP 2010519181A5 JP 2009548468 A JP2009548468 A JP 2009548468A JP 2009548468 A JP2009548468 A JP 2009548468A JP 2010519181 A5 JP2010519181 A5 JP 2010519181A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- amino
- alkyl
- heteroaryl
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- -1 4- (2- (2-propylpyridin-4-yl) thiazol-4-yl) phenyl Chemical group 0.000 claims description 242
- 125000001072 heteroaryl group Chemical group 0.000 claims description 160
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 160
- 150000001408 amides Chemical class 0.000 claims description 144
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 120
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 120
- 125000000304 alkynyl group Chemical group 0.000 claims description 120
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 102
- 239000000203 mixture Substances 0.000 claims description 99
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 96
- 125000005418 aryl aryl group Chemical group 0.000 claims description 96
- 229910052757 nitrogen Inorganic materials 0.000 claims description 74
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 72
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 72
- 125000001475 halogen functional group Chemical group 0.000 claims description 72
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 72
- 238000006467 substitution reaction Methods 0.000 claims description 64
- 125000003118 aryl group Chemical group 0.000 claims description 52
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 48
- 229910052717 sulfur Inorganic materials 0.000 claims description 48
- 239000011593 sulfur Substances 0.000 claims description 48
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 46
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 229910052760 oxygen Inorganic materials 0.000 claims description 26
- 239000001301 oxygen Substances 0.000 claims description 26
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 26
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical group [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 24
- 125000005024 alkenyl aryl group Chemical group 0.000 claims description 24
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 24
- 150000008052 alkyl sulfonates Chemical group 0.000 claims description 24
- 125000005025 alkynylaryl group Chemical group 0.000 claims description 24
- 125000004367 cycloalkylaryl group Chemical group 0.000 claims description 24
- 150000003457 sulfones Chemical group 0.000 claims description 24
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical group OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 24
- 150000003462 sulfoxides Chemical group 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 18
- 238000002560 therapeutic procedure Methods 0.000 claims description 17
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 16
- 150000001721 carbon Chemical class 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 16
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 14
- 208000008466 Metabolic Disease Diseases 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 12
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 12
- 125000003107 substituted aryl group Chemical group 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 10
- 239000011780 sodium chloride Substances 0.000 claims description 10
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims description 10
- UIQZGUHSTKZKGY-UHFFFAOYSA-N 4-(2-methoxyphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C(=CC=CC=2)OC)=C1 UIQZGUHSTKZKGY-UHFFFAOYSA-N 0.000 claims description 8
- GOKVUOGCZQKXQS-UHFFFAOYSA-N N-propan-2-yl-4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]aniline Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NC(C)C)=CC=2)=C1 GOKVUOGCZQKXQS-UHFFFAOYSA-N 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 8
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 8
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 8
- HFSRZCFVFOUVKU-UHFFFAOYSA-N 3-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenol Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=C(O)C=CC=2)=C1 HFSRZCFVFOUVKU-UHFFFAOYSA-N 0.000 claims description 6
- VYYMYRPKZDHXOO-UHFFFAOYSA-N 4-(2,4-difluorophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C(=CC(F)=CC=2)F)=C1 VYYMYRPKZDHXOO-UHFFFAOYSA-N 0.000 claims description 6
- OXTHFCVLLNTNRZ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-(3,4-dimethoxyphenyl)-1,3-thiazole Chemical compound C1=C(OC)C(OC)=CC=C1C1=NC(C=2C=CC(Cl)=CC=2)=CS1 OXTHFCVLLNTNRZ-UHFFFAOYSA-N 0.000 claims description 6
- QKFIOIFLEOWEFH-UHFFFAOYSA-N 4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]aniline Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(N)=CC=2)=C1 QKFIOIFLEOWEFH-UHFFFAOYSA-N 0.000 claims description 6
- UBVHKWIDYFYLLR-UHFFFAOYSA-N 4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenol Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(O)=CC=2)=C1 UBVHKWIDYFYLLR-UHFFFAOYSA-N 0.000 claims description 6
- LZVRJUVBTQEBPU-UHFFFAOYSA-N N-[4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenyl]acetamide Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NC(C)=O)=CC=2)=C1 LZVRJUVBTQEBPU-UHFFFAOYSA-N 0.000 claims description 6
- 208000008589 Obesity Diseases 0.000 claims description 6
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 235000020824 obesity Nutrition 0.000 claims description 6
- 230000037361 pathway Effects 0.000 claims description 6
- NJCQOVROHVLZKB-UHFFFAOYSA-N 2-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenol Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C(=CC=CC=2)O)=C1 NJCQOVROHVLZKB-UHFFFAOYSA-N 0.000 claims description 4
- UBPWKUGAPZVWQE-UHFFFAOYSA-N 4-(3-methoxyphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=C(OC)C=CC=2)=C1 UBPWKUGAPZVWQE-UHFFFAOYSA-N 0.000 claims description 4
- VJLPOVIHSNLTQX-UHFFFAOYSA-N 4-(4-bromophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(Br)=CC=2)=C1 VJLPOVIHSNLTQX-UHFFFAOYSA-N 0.000 claims description 4
- RJCFNQZVFUMORB-UHFFFAOYSA-N 4-(4-methylphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole;hydrobromide Chemical compound Br.C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(C)=CC=2)=C1 RJCFNQZVFUMORB-UHFFFAOYSA-N 0.000 claims description 4
- 206010012601 Diabetes mellitus Diseases 0.000 claims description 4
- OWAXXHRQPWGNTG-UHFFFAOYSA-N N-[4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenyl]methanesulfonamide Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NS(C)(=O)=O)=CC=2)=C1 OWAXXHRQPWGNTG-UHFFFAOYSA-N 0.000 claims description 4
- BAQOAQCINMPNGC-UHFFFAOYSA-N N-benzyl-4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]aniline Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NCC=3C=CC=CC=3)=CC=2)=C1 BAQOAQCINMPNGC-UHFFFAOYSA-N 0.000 claims description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atoms Chemical group 0.000 claims description 4
- 230000037213 diet Effects 0.000 claims description 4
- 235000005911 diet Nutrition 0.000 claims description 4
- 238000002651 drug therapy Methods 0.000 claims description 4
- 238000000554 physical therapy Methods 0.000 claims description 4
- 101710043414 SREBF1 Proteins 0.000 claims description 3
- 102100014920 SREBF1 Human genes 0.000 claims description 3
- 101710043417 SREBF2 Proteins 0.000 claims description 3
- 102100014921 SREBF2 Human genes 0.000 claims description 3
- 230000002401 inhibitory effect Effects 0.000 claims description 3
- GGNIKGLUPSHSBV-UHFFFAOYSA-N 1,3-thiazole-5-carboxamide Chemical compound NC(=O)C1=CN=CS1 GGNIKGLUPSHSBV-UHFFFAOYSA-N 0.000 claims description 2
- OHCBMYMUPIIOHV-UHFFFAOYSA-N 2-(2-propylpyridin-4-yl)-4-thiophen-2-yl-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2SC=CC=2)=C1 OHCBMYMUPIIOHV-UHFFFAOYSA-N 0.000 claims description 2
- CMUTYHWKASVOFO-UHFFFAOYSA-N 4-(2-chlorophenyl)-2-phenyl-1,3-thiazole Chemical compound ClC1=CC=CC=C1C1=CSC(C=2C=CC=CC=2)=N1 CMUTYHWKASVOFO-UHFFFAOYSA-N 0.000 claims description 2
- FYCNBEGGRGPPBC-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=C(Cl)C(Cl)=CC=2)=C1 FYCNBEGGRGPPBC-UHFFFAOYSA-N 0.000 claims description 2
- SXQHWZZWEJUUDI-UHFFFAOYSA-N 4-(4-bromophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC(CCC)=CC(C=2SC(=C(N=2)C=2C=CC(Br)=CC=2)C(O)=O)=C1 SXQHWZZWEJUUDI-UHFFFAOYSA-N 0.000 claims description 2
- ZNMIYSUPNOQXPL-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-(2-ethylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CC)=CC(C=2SC=C(N=2)C=2C=CC(Cl)=CC=2)=C1 ZNMIYSUPNOQXPL-UHFFFAOYSA-N 0.000 claims description 2
- QAIDAYZZJYOOJH-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(Cl)=CC=2)=C1 QAIDAYZZJYOOJH-UHFFFAOYSA-N 0.000 claims description 2
- QKZNZFDVQQFDLV-UHFFFAOYSA-N 4-(4-fluorophenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(F)=CC=2)=C1 QKZNZFDVQQFDLV-UHFFFAOYSA-N 0.000 claims description 2
- UVUVXLDIFQWHBY-UHFFFAOYSA-N 4-(4-methoxyphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(OC)=CC=2)=C1 UVUVXLDIFQWHBY-UHFFFAOYSA-N 0.000 claims description 2
- SKHJXKHKCQDSOX-UHFFFAOYSA-N 4-(4-methoxyphenyl)-2-pyridin-4-yl-1,3-thiazole Chemical compound C1=CC(OC)=CC=C1C1=CSC(C=2C=CN=CC=2)=N1 SKHJXKHKCQDSOX-UHFFFAOYSA-N 0.000 claims description 2
- FCBWDNYFAULZCS-UHFFFAOYSA-N 4-(4-methylphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC(CCC)=CC(C=2SC(=C(N=2)C=2C=CC(C)=CC=2)C(O)=O)=C1 FCBWDNYFAULZCS-UHFFFAOYSA-N 0.000 claims description 2
- RGQZKXSQOVPMHZ-UHFFFAOYSA-N 4-(4-methylphenyl)-2-phenyl-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=CSC(C=2C=CC=CC=2)=N1 RGQZKXSQOVPMHZ-UHFFFAOYSA-N 0.000 claims description 2
- WHGCQPQZQBCMTM-UHFFFAOYSA-N 4-(4-methylphenyl)-2-pyridin-4-yl-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=CSC(C=2C=CN=CC=2)=N1 WHGCQPQZQBCMTM-UHFFFAOYSA-N 0.000 claims description 2
- PSIIDDOTVGEEHU-UHFFFAOYSA-N 4-methyl-N-[4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenyl]benzenesulfonamide Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NS(=O)(=O)C=3C=CC(C)=CC=3)=CC=2)=C1 PSIIDDOTVGEEHU-UHFFFAOYSA-N 0.000 claims description 2
- YDCHGQNVVRRQLA-UHFFFAOYSA-N 4-phenyl-2-(2-propylpyridin-4-yl)-1,3-thiazole Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC=CC=2)=C1 YDCHGQNVVRRQLA-UHFFFAOYSA-N 0.000 claims description 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 208000008787 Cardiovascular Disease Diseases 0.000 claims description 2
- 239000005973 Carvone Substances 0.000 claims description 2
- 208000004930 Fatty Liver Diseases 0.000 claims description 2
- 206010019708 Hepatic steatosis Diseases 0.000 claims description 2
- 206010062060 Hyperlipidaemia Diseases 0.000 claims description 2
- 206010020772 Hypertension Diseases 0.000 claims description 2
- FMHQDMWHNYEVMV-UHFFFAOYSA-N N-(cyclopropylmethyl)-4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]aniline Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NCC3CC3)=CC=2)=C1 FMHQDMWHNYEVMV-UHFFFAOYSA-N 0.000 claims description 2
- RNMWGJXKUNRKSO-UHFFFAOYSA-N N-[4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenyl]quinoline-8-sulfonamide Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NS(=O)(=O)C=3C4=NC=CC=C4C=CC=3)=CC=2)=C1 RNMWGJXKUNRKSO-UHFFFAOYSA-N 0.000 claims description 2
- 206010060862 Prostate cancer Diseases 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 230000003542 behavioural Effects 0.000 claims description 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- JKELRKVYOHHCPO-UHFFFAOYSA-N methyl 4-(4-methylphenyl)-2-(2-propylpyridin-4-yl)-1,3-thiazole-5-carboxylate Chemical compound C1=NC(CCC)=CC(C=2SC(=C(N=2)C=2C=CC(C)=CC=2)C(=O)OC)=C1 JKELRKVYOHHCPO-UHFFFAOYSA-N 0.000 claims description 2
- 239000000546 pharmaceutic aid Substances 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 231100000240 steatosis hepatitis Toxicity 0.000 claims description 2
- 238000001356 surgical procedure Methods 0.000 claims description 2
- ATBCYIUPIXGWGZ-UHFFFAOYSA-N tert-butyl N-[4-[2-(2-propylpyridin-4-yl)-1,3-thiazol-4-yl]phenyl]carbamate Chemical compound C1=NC(CCC)=CC(C=2SC=C(N=2)C=2C=CC(NC(=O)OC(C)(C)C)=CC=2)=C1 ATBCYIUPIXGWGZ-UHFFFAOYSA-N 0.000 claims description 2
- KEAAJYWVSDRJIV-UHFFFAOYSA-N 4-phenyl-2-(2-propylpyridin-4-yl)-1,3-thiazole-5-carboxylic acid Chemical compound C1=NC(CCC)=CC(C=2SC(=C(N=2)C=2C=CC=CC=2)C(O)=O)=C1 KEAAJYWVSDRJIV-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 230000001225 therapeutic Effects 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88799407P | 2007-02-02 | 2007-02-02 | |
| US60/887,994 | 2007-02-02 | ||
| US1231007P | 2007-12-07 | 2007-12-07 | |
| US61/012,310 | 2007-12-07 | ||
| PCT/US2008/052778 WO2008097835A2 (en) | 2007-02-02 | 2008-02-01 | Compositions and methods for the treatment of metabolic disorders |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014005460A Division JP5878937B2 (ja) | 2007-02-02 | 2014-01-15 | 代謝障害を処置するための組成物および方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010519181A JP2010519181A (ja) | 2010-06-03 |
| JP2010519181A5 true JP2010519181A5 (ru) | 2012-03-08 |
| JP5461197B2 JP5461197B2 (ja) | 2014-04-02 |
Family
ID=39682342
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009548468A Active JP5461197B2 (ja) | 2007-02-02 | 2008-02-01 | 代謝障害を処置するための組成物および方法 |
| JP2014005460A Expired - Fee Related JP5878937B2 (ja) | 2007-02-02 | 2014-01-15 | 代謝障害を処置するための組成物および方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014005460A Expired - Fee Related JP5878937B2 (ja) | 2007-02-02 | 2014-01-15 | 代謝障害を処置するための組成物および方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US8207196B2 (ru) |
| EP (1) | EP2120580B1 (ru) |
| JP (2) | JP5461197B2 (ru) |
| CN (1) | CN101674730B (ru) |
| AU (1) | AU2008214095B2 (ru) |
| CA (1) | CA2677264C (ru) |
| WO (1) | WO2008097835A2 (ru) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9233941B2 (en) * | 2007-02-02 | 2016-01-12 | Baylor College Of Medicine | Methods and compositions for the treatment of body weight related disorders |
| US9212179B2 (en) * | 2007-02-02 | 2015-12-15 | Baylor College Of Medicine | Compositions and methods for the treatment of metabolic disorders |
| WO2008097835A2 (en) * | 2007-02-02 | 2008-08-14 | Baylor College Of Medicine | Compositions and methods for the treatment of metabolic disorders |
| US9187485B2 (en) * | 2007-02-02 | 2015-11-17 | Baylor College Of Medicine | Methods and compositions for the treatment of cancer and related hyperproliferative disorders |
| EP2250160B1 (en) | 2008-01-25 | 2015-11-11 | Millennium Pharmaceuticals, Inc. | Thiophenes and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors |
| UA103319C2 (en) | 2008-05-06 | 2013-10-10 | Глаксосмитклайн Ллк | Thiazole- and oxazole-benzene sulfonamide compounds |
| CN102395585A (zh) | 2009-01-30 | 2012-03-28 | 米伦纽姆医药公司 | 杂芳基化合物和其作为pi3k抑制剂的用途 |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| WO2011140296A1 (en) | 2010-05-05 | 2011-11-10 | Infinity Pharmaceuticals | Triazoles as inhibitors of fatty acid synthase |
| EP3159331A1 (en) | 2010-05-05 | 2017-04-26 | Infinity Pharmaceuticals, Inc. | Tetrazolones as inhibitors of fatty acid synthase |
| JP2013533318A (ja) | 2010-08-11 | 2013-08-22 | ミレニアム ファーマシューティカルズ， インコーポレイテッド | ヘテロアリールおよびその使用 |
| WO2012021611A1 (en) | 2010-08-11 | 2012-02-16 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| AR082665A1 (es) | 2010-08-11 | 2012-12-26 | Millennium Pharm Inc | Derivados heteroarilicos inhibidores de quinasas pi3k, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos proliferativos, inflamatorios y/o cardiovasculares |
| EP2616441B1 (en) * | 2010-09-17 | 2019-08-07 | Purdue Pharma L.P. | Pyridine compounds and the uses thereof |
| EP2625294A4 (en) * | 2010-10-07 | 2014-03-26 | Univ Columbia | METHOD OF TREATING CANCER WITH P53 MUTATION |
| SG189396A1 (en) | 2010-10-13 | 2013-05-31 | Millennium Pharm Inc | Heteroaryls and uses thereof |
| CA2825306C (en) * | 2011-01-25 | 2019-02-26 | The Regents Of The University Of Michigan | Bcl-2/bcl-xl inhibitors and therapeutic methods using the same |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
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